ID: ALA4470351

Max Phase: Preclinical

Molecular Formula: C26H36N2O4

Molecular Weight: 440.58

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  C/C1=C\CC[C@@]2(C)O[C@@H]2[C@H]2OC(=O)[C@@H](CN3CCC(OCc4cccnc4)CC3)[C@@H]2CC1

Standard InChI:  InChI=1S/C26H36N2O4/c1-18-5-3-11-26(2)24(32-26)23-21(8-7-18)22(25(29)31-23)16-28-13-9-20(10-14-28)30-17-19-6-4-12-27-15-19/h4-6,12,15,20-24H,3,7-11,13-14,16-17H2,1-2H3/b18-5+/t21-,22-,23-,24+,26+/m0/s1

Standard InChI Key:  UDAFFELWFSKYCY-BRLGVLDSSA-N

Associated Targets(Human)

MEC1 72 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Properties

Molecular Weight: 440.58Molecular Weight (Monoisotopic): 440.2675AlogP: 3.90#Rotatable Bonds: 5
Polar Surface Area: 64.19Molecular Species: BASEHBA: 6HBD: 0
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 9.08CX LogP: 2.83CX LogD: 1.14
Aromatic Rings: 1Heavy Atoms: 32QED Weighted: 0.39Np Likeness Score: 1.20

References

1. Li X, Payne DT, Ampolu B, Bland N, Brown JT, Dutton MJ, Fitton CA, Gulliver A, Hale L, Hamza D, Jones G, Lane R, Leach AG, Male L, Merisor EG, Morton MJ, Quy AS, Roberts R, Scarll R, Schulz-Utermoehl T, Stankovic T, Stevenson B, Fossey JS, Agathanggelou A..  (2019)  Derivatisation of parthenolide to address chemoresistant chronic lymphocytic leukaemia.,  10  (8): [PMID:32952998] [10.1039/C9MD00297A]

Source